نتایج جستجو برای: systemic disease

تعداد نتایج: 1605750  

نخعی, شهربانو, طلاچیان, الهام ,

ABSTRACT Kawasaki disease is an acute, febrile, systemic disease of unknown etiology which principally affects young children. Gallbladder hydrops is of rare complications of this disease. It appears that hydrops occurs more common in older children. The diagnosis is suggested by abdominal symptoms and abnormal results of liver function tests and confirmed by ultrasonography. Treatment is suppo...

 شفیعه موثقی, , سیدرضا نجفی زاده, , عبدالرحمن رستمیان, , علی خلوت, , محمد سبزیکاریان, , کیاندخت کریمیان, ,

Background: To evaluate the possibility that prolactin is involved in the pathogenesis and flare-up of systemic lupus erythematosus (SLE).Methods: In this cross-sectional study we determined serum prolactin levels in sixty (60) serum samples from sixty patients diagnosed with SLE by the criteria of the American College of Rheumatology (ACR). All patients were females between 13-64 years of age....

Malignant peritoneal mesothelioma (MPM) is a malignancy that arises from the mesothelial lining of the abdominal cavity and largely manifests as a diffuse process. There are two hallmark features of MPM. First, MPM may progress and present itself diversely among patients. While some patients may endure a quick tumor progression that is refractory to seemingly successful initial therapeutic cyto...

Journal: :medical journal of islamic republic of iran 0
a banihashem from the departments of pediatrics ghaem hospital, mashhad university of medical sciences, mashhad, islamic republic of iran. t ghiassi from the departments of pathology, ghaem hospital, mashhad university of medical sciences, mashhad, islamic republic of iran. s zabihyan

malignant histiocytosis (mh) is a rare hematologic malignancy, especially in the first decade of life. the disease is clinically characterized by fever, hepatosplenomegaly, lymphadenopathy, pancytopenia and jaundice, and histologically by systemic proliferation of malignant histiocytes and hemophagocytosis. the prognosis is poor and often the diagnosis is not made before death. because of the r...

A BANIHASHEM, S ZABIHYAN, T GHIASSI,

Malignant histiocytosis (MH) is a rare hematologic malignancy, especially in the first decade of life. The disease is clinically characterized by fever, hepatosplenomegaly, lymphadenopathy, pancytopenia and jaundice, and histologically by systemic proliferation of malignant histiocytes and hemophagocytosis. The prognosis is poor and often the diagnosis is not made before death. Because of ...

Journal: :emergency journal 0
tahmine biazar infectious diseases and tropical medicine research center,babol university of medical sciences, babol, iran. mehran shokri infectious diseases and tropical medicine research center,babol university of medical sciences, babol, iran. hajar hosseinnia clinical research development unit, rouhani hospital,babol university of medical science.babol,iran. masomeh bayani infectious diseases and tropical medicine research center,babol university of medical sciences, babol, iran.

orf is a mucocutaneous disease that occurs when non-intact skin comes into contact with contaminated sheep saliva. the lesions may complicate to lymphangitis or secondary bacterial infection, but systemic complications such as erythema multiforme, maculopapular rash, and generalized lymphadenopathy are rare. in this paper, we present two cases of erythema multiforme following orf disease.

Background: Hughes-Stovin Syndrome (HSS) is a rare clinical disorder characterized by deep venous thrombosis and multiple pulmonary and/or bronchial aneurysms. Aneurysms in systemic circulation can also be seen. Case presentation: We report the first case of HSS with aortic aneurysm in a 55-year-old man who initially presented with deep venous thrombosis. The diagnosis of HSS revealing Beh&cce...

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